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Striatal dopamine release after prefrontal repetitive transcranial magnetic stimulation in major depression: Preliminary results of a dynamic [123I] IBZM SPECT study

磁刺激 多巴胺能 多巴胺 前额叶皮质 心理学 神经科学 刺激 抗抑郁药 多巴胺受体D2 海马体 认知
作者
Oliver Pogarell,Walter Koch,Gabriele Pöpperl,Klaus Tatsch,Franziska Jakob,Peter Zwanzger,Christoph Mulert,Rainer Rupprecht,Hans‐Jürgen Möller,Ulrich Hegerl,Frank Padberg
出处
期刊:Journal of Psychiatric Research [Elsevier BV]
卷期号:40 (4): 307-314 被引量:165
标识
DOI:10.1016/j.jpsychires.2005.09.001
摘要

Though there is considerable evidence that prefrontal repetitive transcranial magnetic stimulation (rTMS) exerts antidepressant effects, the neurobiological action of rTMS in patients with depression is poorly understood. Preclinical studies in animals and humans have demonstrated that prefrontal rTMS can induce dopamine release in mesostriatal and mesolimbic regions. We therefore investigated whether rTMS also modulates striatal dopaminergic neurotransmission in depressed patients using a dynamic [123I] iodobenzamide (IBZM) single photon emission computed tomography (SPECT) approach. Five patients with a major depressive episode (DSM-IV) underwent an acute 10 Hz rTMS challenge with 3000 stimuli over the left dorsolateral prefrontal cortex during an [123I] IBZM-SPECT bolus and constant infusion protocol. In four subjects the protocol was repeated after a three week rTMS standard treatment. Striatal IBZM binding to dopamine D2 receptors was assessed with a region-of-interest (ROI) technique. The change in striatal IBZM binding after the rTMS challenge was regarded as measure of change in endogenous striatal dopamine. Data of nine SPECT investigations showed a significant reduction by 9.6 ± 6.2% in IBZM binding to striatal dopamine D2 receptors after rTMS challenge compared to baseline (p = 0.01, Wilcoxon test). In this preliminary study, the reduction of IBZM binding observed after rTMS challenge is suggestive of a release in endogenous dopamine induced by prefrontal rTMS. In future, this approach can be used to differentiate specific and non-specific reward-related effects of rTMS on dopaminergic neurotransmission.
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